Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | Ethyl 3-(4-chlorophenyl)-2,4-dioxo-3-azabicyclo[3.1.0]hexane-6-carboxylate | HCID 3120146 | — |
| Reactant | 1-(4-Amino-3-fluorophenyl)pyridin-2-one | HCID 22181548 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66880761 | HCID 66880761 | 24% |
Reaction Steps
A solution of 7 g (34 mmol) of 1-(4-amino-3-fluoro-phenyl)-1H-pyridin-2-one (prepared according to C. F. Bigge et al., patent application WO 2003045912) in 25 ml of THF was cooled to −78° C. and treated dropwise with 41 ml of a 1M lithium bis(trimethylsilyl)amide-solution in THF and stirred for 30 min. To this solution 9.5 g (32 mmol) of (1RS, 5SR, 6R)-3-(4-chloro-phenyl)-2,4-dioxo-3-aza-bicyclo[3.1.0]hexane-6-carboxylic acid ethyl ester were added portionwise and the mixture was allowed to reach room temperature within a few hours. The mixture was then poured into a diluted aqueous HCl-solution (ca. 0.2 M) and extracted with AcOEt. The combined organic phases were dried with Na2SO4. Evaporation of the solvent and chromatography on silica gel with dichloromethane and then with a gradient of dichloromethane/MeOH from 98:2 to 95:5 gave 4.1 g (24%) of the title compound. Light brown solid. MS: 496 (M−H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07501413B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-f0500249342f437da4972a50b3c26b60 |
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| Source note | uspto-grants-2009_03 |
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